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Personal Genomics, Bioinformatics, and Variomics

Bhak J, Ghang H, Reja R, Kim S

  • KMID: 2166415
  • Genomics Inform.
  • 2008 Dec;6(4):161-165.
In 2008 at least five complete genome sequences are available. It is known that there are over 15,000,000 genetic variants, called SNPs, in the dbSNP database. The cost of full...
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Multilevel Analysis of the Relationship Between Prescribing Institutions and Medication Adherence Among Patients With Hypertension and Diabetes in Korea

Ghang H, Lee J

Objectives: This study investigated the relationship between prescribing institutions and medication adherence among patients newly diagnosed with hypertension and diabetes. Methods: This study investigated patients with new prescriptions for hypertension and...
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How Many SNPs Should Be Used for the Human Phylogeny of Highly Related Ethnicities? A Case of Pan Asian 63 Ethnicities

Ghang H, Han Y, Jeong S, Bhak J, Lee S, Kim TH, Kim C, Kim S, Al-Mulla F, Youn CH, Yoo HS, The HUGO Pan-Asian SNP Consortium

  • KMID: 2053274
  • Genomics Inform.
  • 2011 Dec;9(4):181-188.
In planning a model-based phylogenic study for highly related ethnic data, the SNP marker number is an important factor to determine for relationship inferences. Genotype frequency data, utilizing a sub...
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A Multilevel Analysis about the Impact of Patient’s Willingness for Discharge on Successful Discharge from Long-term Care Hospitals

Ghang H, Lee Y

Background: Since November 2019, long-term care hospitals have been able to provide patients with discharging programs to support the elderly in the community. This study aimed to identify both patient-...
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